Regulatory manager jobs in Lodi, New Jersey (NJ) State

The individual combines knowledge of scientific, regulatory, and business processes to properly drive the execution of Innovent’s regulatory strategies. Formatting the regulatory documents according to the regulatory agency guidelines. Global Regulatory Affairs Operation（Sr. This position belongs...

My client is a multinational CDMO looking for a Regulatory Affairs Manager to work with the FDA and their client sites to manufacture generic APIs, drug products, and certain med devices. Experienced with the preparation and submission of regulatory documents, including PIND meeting packages, IND...

Manager of Regulatory Affairs Strategy to join their team. Serves as a liaison to FDA and provides strategic input with the regional regulatory leads responsible for ex-US regulatory activities. We are currently partnered with a growing biopharmaceutical company in need of a Manager/Sr. This role...

The Director of Policy and Regulatory Affairs will be responsible for managing Elevate’s relationships and policy positions at PJM, federal and state regulatory agencies, and state legislative bodies. Director of Policy and Regulatory Affairs – PJM Region. The candidate will have a strong knowled...

The incumbent responsible for supporting the development and implementation of regulatory strategies, work closely with the cross functional asset teams to prepare, review and submit regulatory filing documents, manage documentation systems and maintain interactions with regulatory agencies. Expe...

Technical Program Manager will be responsible for leading the management and execution of server platform programs compliance testing throughout the product lifecycle, scoping required compliance testing from product specification definition, and feature scoping through production release and end...

Manages F&B Naturals Regulatory Affairs team and and coordinates with F&B Flavor Regulatory Affairs team to ensure regulatory compliance of Naturals products with corporate guidelines and government regulations. Works independently to provide customers with product regulatory information in accor...

Assesses regulatory pathways for new product platforms and product modifications; develops regulatory strategies and tactical plans for submissions to FDA and other regulatory agencies. Reporting to the Director of Regulatory Affairs, responsible and accountable for developing and implementing so...

Our client is currently seeking a Senior Manager, Regulatory Affairs. Develop and implement global regulatory strategies for investigational and marketed pharmaceutical products. Liaise with FDA and regional regulatory leads; oversee consultants and vendors. Represent regulatory affairs on projec...

The Senior Regulatory Affairs Associate/Manager plays a key role in ensuring compliance with regulatory requirements that govern the development, registration and commercialization of livestock and poultry products (primarily medicated feed additives and water-soluble products) while also providi...

Our client is currently seeking a Senior Manager, Regulatory Affairs Strategy. Responsible for developing and implementing short and long term global regulatory strategies that support the success of investigational and marketed pharmaceutical products throughout their life cycle. Provides regula...

Responsibilities Actively contribute to the development of regulatory strategies for investigational products in Investigational New Drug (IND)/ Clinical Trial Applications (CTA), Biologics Licensing Application (BLAs)/ Marketing Authorization Application (MAA), through evaluating scientific meri...

As the Senior Manager, Regulatory Affairs you will be responsible for the development and execution of US regulatory strategy for projects within an assigned Therapeutic Area (“TA”). Develop and execute US regulatory strategy, with oversight as needed, and in conjunction with Global Regulatory Le...

The person will be responsible for the creation and maintenance of regulatory CMC documents in the controlled document management repository. Work cross functionally to coordinate the preparation of draft responses to technical regulatory questions from health authorities including writing of exp...

Soliant is hiring a chemo pharmacist in Hackensack NJ. ...

Montefiore Medical Center is seeking a Pharmacist for a job in Closter, New Jersey. ...

Montefiore Medical Center is seeking a Pharmacist Manager for a job in Edgewater, New Jersey. All of the medication purchasing decisions are made under the supervision of a NYS licensed pharmacist. ...

Montefiore Medical Center is seeking a Clinic Pharmacist Manager for a job in Edgewater, New Jersey. ...

What are we looking for in our Sr Project/Program Manager?. Manage project interdependencies and implement or make recommendations on mitigation options to upper managementProactively manage changes in project/program scope, identify potential crises, and prepare contingency pla...

Arcadis is seeking a ProjectManager/Project Planner for a large project in New York. Role description:As a Project Manager/Project Planner with direct knowledge of FTA requirements for Project Management Plans and Sub-Plans, you will bring a working knowledge of FTA Oversight Procedures for these...

Our client, a leading manufacturer in the consumer good industry has an excellent opportunity available for a Senior Operations Manager. The Operations Manager will organize daily management and weekly team meetings and drives a culture of safety, quality, delivery and cost control. Work with man...

Globally based engineering client has an immediate need for a Senior IT Project Manager for a very long term contract position (2+ years). ...

For the HR Compliance Specialist position, this role will require creating and maintaining policies and procedures. The position will plan, direct, or coordinate activities for the company to ensure compliance are within ethical and regulatory standards including ACA, HIPAA, and more. Collaborate...

The Director, Regulatory Affairs should have an advanced degree, preferably in the sciences, and have demonstrated application of regulatory expertise by at least 8+ years pharmaceutical industry experience. The Director, Regulatory Affairs is required to have excellent written and oral communica...